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A bronchoalveolar lavage-driven antimicrobial treatment improves survival in hematologic malignancy patients with detected lung infiltrates: A prospective multicenter study of the SEIFEM group.
Marchesi, Francesco; Cattaneo, Chiara; Criscuolo, Marianna; Delia, Mario; Dargenio, Michelina; Del Principe, Maria Ilaria; Spadea, Antonio; Fracchiolla, Nicola Stefano; Melillo, Lorella; Perruccio, Katia; Alati, Caterina; Russo, Domenico; Garzia, Mariagrazia; Brociner, Marco; Cefalo, Mariagiovanna; Armiento, Daniele; Cesaro, Simone; Decembrino, Nunzia; Mengarelli, Andrea; Tumbarello, Mario; Busca, Alessandro; Pagano, Livio.
Afiliação
  • Marchesi F; Hematology and Stem Cell Transplant Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
  • Cattaneo C; Hematology Division, ASST-Spedali Civili di Brescia, Brescia, Italy.
  • Criscuolo M; Fondazione Policlinico Universitario Agostino Gemelli - IRCCS, Rome, Italy.
  • Delia M; Hematology and Bone Marrow Transplantation Unit, Department of Emergency and Organ Transplantation, University of Bari, Bari, Italy.
  • Dargenio M; Hematology and Stem Cell Transplantation Unit, 'Vito Fazzi' Hospital, Lecce, Italy.
  • Del Principe MI; Hematology, Department of Biomedicine and Prevention, Tor Vergata University, Rome, Italy.
  • Spadea A; Hematology and Stem Cell Transplant Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
  • Fracchiolla NS; Hematology Unit, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
  • Melillo L; UO of Hematology, Foundation IRCSS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo, Italy.
  • Perruccio K; Pediatric Hematology Oncology, University Hospital Santa Maria della Misericordia, Perugia, Italy.
  • Alati C; Hematology Unit, Bianchi-Melacrino-Morelli Hospital, Reggio Calabria, Italy.
  • Russo D; Bone Marrow Transplant Unit, University of Brescia and ASST-Spedali Civili, Brescia, Italy.
  • Garzia M; Hematology, San Camillo-Forlanini Hospital, Rome, Italy.
  • Brociner M; Division of Hematology, Foundation IRCCS Policlinico San Matteo, University of Pavia, Pavia, Italy.
  • Cefalo M; Hematology, San Eugenio Hospital, Rome, Italy.
  • Armiento D; Hematology and Stem Cell Transplantation Unit, University Campus Bio-Medico, Rome, Italy.
  • Cesaro S; Pediatric Hematology Oncology, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
  • Decembrino N; Pediatric Hematology Oncology, IRCCS Policlinico San Matteo, University of Pavia, Pavia, Italy.
  • Mengarelli A; Hematology and Stem Cell Transplant Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
  • Tumbarello M; Fondazione Policlinico Universitario Agostino Gemelli - IRCCS, Rome, Italy.
  • Busca A; Istituto di Malattie Infettive, Università Cattolica del Sacro Cuore, Rome, Italy.
  • Pagano L; Stem Cell Transplant Center, AOU Citta' della Salute e Della Scienza, Turin, Italy.
Am J Hematol ; 94(10): 1104-1112, 2019 10.
Article em En | MEDLINE | ID: mdl-31321791
ABSTRACT
Bronchoalveolar lavage (BAL) is recommended for diagnosing lung infiltrates (LI) in patients with hematologic malignancy (HM). Prospective data on the impact of BAL on survival are still lacking. We conducted a prospective observational study on patients who performed BAL for LI among 3055 HM patients hospitalized from January to September 2018. The BAL was performed in 145 out of 434 patients who developed LI, at a median time of four days from LI detection. The median age was 60 (1-83). Most patients had an acute myeloid leukemia/myelodisplastic syndrome (81), followed by lymphoma (41), acute lymphoblastic leukemia (27), and other types of HM (36). A putative causal agent was detected in 111 cases (76%), and in 89 cases (61%) the BAL results provided guidance to antimicrobial treatment. We observed a significantly improved outcome of LI at day +30 in patients who could receive a BAL-driven antimicrobial treatment (improvement/resolution rate 71% vs 55%; P = .04). Moreover, we observed a significantly improved outcome in 120-day overall survival (120d-OS) (78% vs 59%; P = .009) and 120-day attributable mortality (120d-AM) (11% vs 30%; P = 0.003) for patients who could receive a BAL-driven treatment. The multivariate analysis showed that BAL-driven antimicrobial treatment was significantly associated with better 120d-OS and lower 120d-AM. We did not observe any severe adverse events. In conclusion BAL allows detection of a putative agent of LI in about 75% of cases, it is feasible and well tolerated in most cases, demonstrating that a BAL-driven antimicrobial treatment allows improvement of clinical outcome and survival.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumonia Viral / Líquidos Corporais / Pneumonia Bacteriana / Lavagem Broncoalveolar / Neoplasias Hematológicas / Pulmão / Pneumopatias Fúngicas / Anti-Infecciosos Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumonia Viral / Líquidos Corporais / Pneumonia Bacteriana / Lavagem Broncoalveolar / Neoplasias Hematológicas / Pulmão / Pneumopatias Fúngicas / Anti-Infecciosos Tipo de estudo: Clinical_trials / Diagnostic_studies / Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Aged80 / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article